Covance

REGULATORY CLINICAL TRIAL SUBMISSIONS SPECIALIST, ITALY

Company
Covance
Location
Milan, Italy
Salary
Competitive
Posted
17 Dec 2020
Closes
16 Jan 2021
Ref
10024_56430
Discipline
Regulatory Affairs
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)


THE JOB

Covance Italy is looking for a Regulatory Submissions Specialist .

A full time job, you can work home-based , anywhere in Italy . If you prefer an office, our premises are in Milan.

We will trust you to be the Covance´s primary contact with the AIFA and the Istituto Superiore di Sanità (ISS), and the main pillar of your job will be taking the ownership of complex Clinical Trial Applications (CTA) to the Italian Regulatory Authorities.

We want you to quickly become the CTA Country Expert, and a measure for you to know you are being successful here is how soon you can independently provide a consultative approach on local regulations to our Global Regulatory Leaders and Start-up teams.

And there is an international flavor to this job, as the Italian regulatory team is highly regarded within the organization, and you may find yourself supporting Regulatory Submissions in Germany, France, UK, Benelux or the Nordics.

COVANCE

With all the uncertainty in the world, your job stability should not be a concern.

Covance have supported the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today.

Join us and see why Covance are uniquely positioned to offer you not only a job, but a stable, long-term international career, and why more than 90% of the top 20 global pharmaceutical companies are repeat customers.
Education/Qualifications:
University/College degree (life Science preferred), or certification in a health related profession from an accredited institution (e.g. nursing, medical or lab technology, etc.)
Experience:
IS THIS YOU?

You´ve guessed it: for this job we need you to bring hands-on experience independently managing Clinical Trial Applications submissions in Italy. Our ideal candidate has at least 1 year experience preparing CTA submissions at a Contract Research Organization (CRO) environment.

Knowledge of other EU countries Submissions Applications is beneficial, but Italian Regulatory - CTA submissions background is a must for our team.

Business proficiency in English - both spoken and written is needed.